[Cloverleaf syndrome. Presentation of four cases (author's transl)]

A V Fajardo Camona¹, I Pascual Castroviejo

¹Servicio de Neurología de la Clínica Infantil "La Paz", Madrid (Universidad Autónoma).

|January 1, 1976

Abstract:

Four cases of cloverleaf syndrome are presented. Authors agree with recent opinions that this alteration is a significant indication that may be presented by diseases which develop craniosynostosis very early (acrocephalosyndactyly, thanatophoric, dwarfism, Crouzon's disease, etc.). Etiopathogenic considerations are made about morphology and prognosis in this disease of unknown etiology.

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

[Brain stem tumors associated with neurofibromatosis type 1. Presentation of 20 infantile patients].

Neurologia (Barcelona, Spain)·2007

[Malformations of cortical development and their clinical repercussions in a series of 144 cases].

Revista de neurologia·2003

[Joubert syndrome. Report of four cases with a favourable evolution].

Revista de neurologia·2002

[The importance of the identification of the spaces of Virchow-Robin. A report of four cases].

Revista de neurologia·2002

Adolescent myopathic presentation in two sisters with very long-chain acyl-CoA dehydrogenase deficiency.

Journal of inherited metabolic disease·1999

[Scleroderma en coup de sabre with intracranial involvement. A case report].

Neurologia (Barcelona, Spain)·1997

See all related articles

Related Experiment Videos

[Cloverleaf syndrome. Presentation of four cases (author's transl)]

Related Concept Videos

[Brain stem tumors associated with neurofibromatosis type 1. Presentation of 20 infantile patients].

[Malformations of cortical development and their clinical repercussions in a series of 144 cases].

[Joubert syndrome. Report of four cases with a favourable evolution].

[The importance of the identification of the spaces of Virchow-Robin. A report of four cases].

Adolescent myopathic presentation in two sisters with very long-chain acyl-CoA dehydrogenase deficiency.

[Scleroderma en coup de sabre with intracranial involvement. A case report].

[Langerhans' cell histiocytosis: various manifestations with the same histopathologic base].

[External ventricular assist devices as circulatory support in patients with dilated cardiomyopathy].

[Comparison of the epidemiological characteristics of neural tube defects classified according to failure of the different points of closure].

[Cutaneous colonization by Malassezia spp. in neonates].

[Balloon valvoplasty for critical aortic valve stenosis in neonates].

[Childhood headache. A diagnostic approach].

[Analysis of risk factors for central diabetes insipidus in Langerhans cell histiocytosis].

Subjective experiences of catatonia in acute psychiatric inpatients: An exploratory study.

[Chinese clinical practice guidelines for standardized diagnosis and treatment of presacral cysts (2026 edition)].

Current Practice and Long-Term Developments in Multidisciplinary Dutch Memory Clinics.

Designing and validating a clinical competency logbook for workplace-based assessment in undergraduate medical education: A foundational psychometric analysis.

Designing an Effective Ambulatory Medicine Clerkship.

Related Experiment Videos

[Cloverleaf syndrome. Presentation of four cases (author's transl)]

Abstract:

Related Concept Videos

Related Articles